How to go From an SDTM Findings Domain to an ADaM-Compliant Analysis Dataset: An Example
Source category: CDISC and Industry Standards
THE COMMUNITY ARCHIVE
CDISC Papers and PresentationsPage 53
Browse practical discussions of clinical data standards, from collected observations to analysis datasets and supporting metadata. Use the more focused ADaM, SDTM and Define-XML collections to follow a particular stage of the workflow.
1,130 papers · Showing 1041–1060
Implementing, Managing and Validating a Clinical Standard
Source category: CDISC and Industry Standards
Author collections: Gene Lightfoot
Initial Investment in CDISC Data Standards in Clinical Organisations
Source category: CDISC and Industry Standards
New CDISC migration strategies and tools: determining the best approach and employing automated data mapping
Source category: CDISC and Industry Standards
SDTM Attribute-Checking Tool
Source category: Posters
Author collections: Ellen Xiao
The Use of Meta Data in Creating, Transforming and Transporting Clinical Data
Source category: CDISC and Industry Standards
Author collections: Gregory Steffens
Traceability between SDTM and ADaM converted analysis datasets
Source category: CDISC and Industry Standards
Author collections: Michael Knoessl
Understanding the define.xml File and Converting It to a Relational Database
Source category: Hands-on Workshops
Author collections: Lex Jansen
Using PROC CONTENTS Output to Perform Quality Control Checks on SDTM Data Sets
Source category: Coders' Corner
A SAS® Programmer�s Guide to Generating Define.xml
Source category: Pharma, Life Sciences and Healthcare
Author collections: Michael Molter
After a new CDISC SDTM version, how to update and manage ADS/SDS DEFINE files at company team level
Source category: Posters
An Evaluation of the ADaM Implementation Guide v1.0 and the Analysis Data Mode v2.1
Source category: CDISC and Industry Standards
Author collections: Chris Price
Backpacking Your Way through CDISC: A Budget-Minded Guide to Basic Concepts and Implementation
Source category: Pharma, Life Sciences and Healthcare
Author collections: Rachel Brown · Jennifer K. Fulton
BRIDGing CDASH to SAS: How Harmonizing Clinical Trial and Healthcare Standards May Impact SAS Users
Source category: CDISC Methodologies for FDA Submissions
CDISC for the Medical Device and Diagnostic Industry: An Update
Source category: CDISC Methodologies for FDA Submissions
Author collections: Carey G. Smoak
CDISC Implementation on a Rheumatoid Arthritis Project Partnership
Source category: CDISC Methodologies for FDA Submissions
Author collections: Patricia L. Gerend · Chris Price · Olivier Leconte · Michelle Zhang
Converting the define.xml to a Relational Database to Enable Printing and Validation
Source category: CDISC and Industry Standards
Author collections: Lex Jansen
Experiences and lessons learned from a first SDTM submission project
Source category: CDISC and Industry Standards
Author collections: Paul Vervuren · Bas van Bakel
From raw data to submission: A metadata-driven, repository-based process of data conversion to CDISC
Source category: CDISC and Industry Standards
Author collections: Dimitri Kutsenko
Generate Define.xml & Define.pdf from Metadata Environment
Source category: CDISC and Industry Standards
Author collections: Rohit Banga